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V L Friedrich

Publications and source records attributed to V L Friedrich.

At least 55 records · Page 3Linked to original sources
PubMed1990

Differential exon expression in myelin basic protein transcripts during central nervous system (CNS) remyelination.

1. In order to characterize some of the molecular events leading to repair of myelin in the adult central nervous system (CNS), we examined the expression of transcripts for myelin basic protein (MBP) during remyelination in the mouse. C57B1/6 mice develop a demyelinating disease when glial cells are selectively infected by the A59 strain of mouse coronavirus. The virus is spontaneously cleared from the mice by 4 weeks postinfection (WPI), a time when remyelination is starting. 2. At 3 WPI total MBP transcripts are decreased by 75% in demyelinating lesions compared to control white matter. Using RNase protection assays and in situ hybridization with probes for particular MBP exons, we detected an increase in MBP transcripts containing exon 2 information, coincident with the earliest histological signs of remyelination. 3. The expression of MBP transcripts containing exon 2 information was first seen clustered in the perinuclear cytoplasm of oligodendrocytes scattered within the lesions. This is reminiscent of the increased levels and perinuclear clustering of MBP transcripts containing exon 2 seen during early developmental myelination. The peak abundance of exon 2-containing transcripts in the lesions was 13-fold that seen in control white matter. At later stages of remyelination, additional forms of MBP transcripts (without exon 2) increased and their distribution was more diffuse. 4. Thus, during remyelination, preforms of MBP transcripts, which are normally present at low levels in the adult CNS, are abundantly expressed and regulated in a manner similar to that observed in developmental myelination.

Animals↗
PubMed1990

In vitro analysis of the oligodendrocyte lineage in mice during demyelination and remyelination.

A demyelinating disease induced in C57B1/6N mice by intracranial injection of a coronavirus (murine hepatitis virus strain A59) is followed by functional recovery and efficient CNS myelin repair. To study the biological properties of the cells involved in this repair process, glial cells were isolated and cultured from spinal cords of these young adult mice during demyelination and remyelination. Using three-color immunofluorescence combined with [3H]thymidine autoradiography, we have analyzed the antigenic phenotype and mitotic potential of individual glial cells. We identified oligodendrocytes with an antibody to galactocerebroside, astrocytes with an antibody to glial fibrillary acidic protein, and oligodendrocyte-type 2 astrocyte (O-2A) progenitor cells with the O4 antibody. Cultures from demyelinated tissue differed in several ways from those of age-matched controls: first, the total number of O-2A lineage cells was strikingly increased; second, the O-2A population consisted of a higher proportion of O4-positive astrocytes and cells of mixed oligodendrocyte-astrocyte phenotype; and third, all the cell types within the O-2A lineage showed enhanced proliferation. This proliferation was not further enhanced by adding PDGF, basic fibroblast growth factor (bFGF), or insulin-like growth factor I (IGF-I) to the defined medium. However, bFGF and IGF-I seemed to influence the fate of O-2A lineage cells in cultures of demyelinated tissue. Basic FGF decreased the percentage of cells expressing galactocerebroside. In contrast, IGF-I increased the relative proportion of oligodendrocytes. Thus, O-2A lineage cells from adult mice display greater phenotypic plasticity and enhanced mitotic potential in response to an episode of demyelination. These properties may be linked to the efficient remyelination achieved in this demyelinating disease.

Animals↗
PubMed1989

Expression of viral and myelin gene transcripts in a murine CNS demyelinating disease caused by a coronavirus.

C57BI/6N mice develop a CNS demyelinating disease when inoculated intracranially at 4 weeks of age with the A59 strain of mouse hepatitis virus (MHV-A59). In order to explore the virus-host interactions, the histological features of the demyelinating disease were correlated with the spatial and temporal distribution of viral transcripts and the expression of oligodendrocyte-specific genes (myelin basic protein, proteolipid protein, myelin-associated glycoprotein, and 2',3' cyclic nucleotide 3'-phosphohydrolase) in the spinal cord of diseased mice. Three distinct phases in the disease were identified. In the first phase, 1 week postinfection (1 WPI), virus replication was widespread in both gray and white matter but was preferentially occurring in glial cells. In the ventral and dorsal root zones where viral transcripts were most abundant, all myelin gene transcripts were decreased before demyelination was seen. During the second phase of the disease (2-3 WPI), viral transcripts decreased in abundance and became restricted to the white matter. Numerous demyelinating lesions were observed and were characterized by inflammatory cells, paucity of oligodendrocytes, and a profound decrease of all myelin gene transcripts. In the third phase of the disease (4-6 WPI) no viral transcripts were detected, and remyelination began. In the lesions and the tissue surrounding them, transcripts of all myelin genes increased to levels above normal. The increased expression of myelin gene transcripts occurred in a synchronized manner and with a cellular distribution reminiscent of that seen in developmental myelination. These molecular events correlated with efficient remyelination and clinical recovery in this murine demyelinating disease.

Animals↗
PubMed1989

Progressive restriction in the distribution of the Hox-1.3 homeodomain protein during embryogenesis.

Expression of the murine homeobox containing gene Hox-1.3 was analyzed in mouse embryos using polyclonal antisera to peptides predicted from cDNA and genomic sequences. At the earliest stage examined, 7.5 days gestation, cell nuclei throughout the three embryonic germ layers and in extraembryonic structures derived from the fertilized ovum were strongly immunoreactive. Rostro-caudal gradients or other patterns of regional differentiation in levels of expression could not be seen. Surrounding maternal tissue showed only weak immunoreactivity. At 8.5 days gestation, immunoreactivity was present in all embryonic structures including neural tube, somites and lateral plate mesoderm, ectoderm and endoderm. Immunoreactivity was progressively restricted thereafter. At 17 days gestation, strong immunoreactivity was largely restricted to the nervous system, both central and peripheral. Spinal cord was well stained, with a dramatic reduction in intensity near the junction of spinal cord and brain. In addition to this overall pattern, enhanced immunoreactivity appeared in limited populations of newly-formed neuroblasts of spinal cord and brain, suggesting that Hox-1.3 might serve to regulate the development of specific types of neurons following cessation of precursor cell mitosis.

Animals↗
PubMed1989

The initial events in myelin synthesis: orientation of proteolipid protein in the plasma membrane of cultured oligodendrocytes.

Proteolipid protein (PLP) is the most abundant transmembrane protein in myelin of the central nervous system. Conflicting models of PLP topology have been generated by computer predictions based on its primary sequence and experiments with purified myelin. We have examined the initial events in myelin synthesis, including the insertion and orientation of PLP in the plasma membrane, in rat oligodendrocytes which express PLP and the other myelin-specific proteins when cultured without neurons (Dubois-Dalcq, M., T. Behar, L. Hudson, and R. A. Lazzarini. 1986. J. Cell Biol. 102:384-392). These cells, identified by the presence of surface galactocerebroside, the major myelin glycolipid, were stained with six anti-peptide antibodies directed against hydrophilic or short hydrophobic sequences of PLP. Five of these anti-peptide antibodies specifically stained living oligodendrocytes. Staining was only seen approximately 10 d after PLP was first detected in the cytoplasm of fixed and permeabilized cells, suggesting that PLP is slowly transported from the RER to the cell surface. The presence of PLP domains on the extracellular surface was also confirmed by cleavage of such domains with proteases and by antibody-dependent complement-mediated lysis of living oligodendrocytes. Our results indicate that PLP has only two transmembrane domains and that the great majority of the protein, including its amino and carboxy termini, is located on the extracellular face of the oligodendrocyte plasma membrane. This disposition of the PLP molecule suggests that homophilic interactions between PLP molecules of apposed extracellular faces may mediate compaction of adjacent bilayers in the myelin sheath.

Amino Acid Sequence↗
PubMed1989

In vivo analysis of glial cell phenotypes during a viral demyelinating disease in mice.

C57 BL/6N mice injected intracranially with the A59 strain of mouse hepatitis virus exhibit extensive viral replication in glial cells of the spinal cord and develop demyelinating lesions followed by virus clearing and remyelination. To study how different glial cell types are affected by the disease process, we combine three-color immunofluorescence labeling with tritiated thymidine autoradiography on 1-micron frozen sections of spinal cord. We use three different glial cell specific antibodies (a) to 2',3' cyclic-nucleotide 3' phosphohydrolase (CNP) expressed by oligodendrocytes, (b) to glial fibrillary acidic protein (GFAP) expressed by astrocytes, and (c) the O4 antibody which binds to O-2A progenitor cells in the rat. These progenitor cells, which give rise to oligodendrocytes and type 2 astrocytes and react with the O4 antibody in the adult central nervous system, were present but rare in the spinal cord of uninfected mice. In contrast, cells with the O-2A progenitor phenotype (O4 + only) were increased in number at one week post viral inoculation (1 WPI) and were the only immunostained cells labeled at that time by a 2-h in vivo pulse of tritiated thymidine. Both GFAP+ only and GFAP+, O4+ astrocytes were also increased in the spinal cord at 1 WPI. Between two and four WPI, the infected spinal cord was characterized by the loss of (CNP+, O4+) oligodendrocytes within demyelinating lesions and the presence of O-2A progenitor cells and O4+, GFAP+ astrocytes, both of which could be labeled with thymidine. As remyelination proceeded, CNP immunostaining returned to near normal and tritiated thymidine injected previously during the demyelinating phase now appeared in CNP+ oligodendrocytes. Thus O4 positive O-2A progenitor cells proliferate early in the course of the demyelinating disease, while CNP positive oligodendrocytes do not. The timing of events suggests that the O-2A progenitors may give rise to new oligodendrocytes and to type 2 astrocytes, both of which are likely to be instrumental in the remyelination process.

2',3'-Cyclic-Nucleotide Phosphodiesterases↗
PubMed1988

Corpus callosum: region-specific effects of sex, early experience and age.

In infancy, rats were provided handling stimulation and compared at 110 and 215 days of age with non-handled controls. Measurements were made of corpus callosum area, perimeter and length; and width measures were taken at 7 points along the longitudinal axis of the callosum. Callosal size was larger in males than in females, even when adjusted for the larger brain weight of the male. At 110 days handling stimulation increased callosal parameters and resulted in a more regular callosum in males, but this effect was no longer apparent by 215 days. Within the callosum, region-specific effects were found, suggesting that certain callosal fiber populations were involved. Handled males have previously been shown to be more lateralized than non-handled males; thus at least in this experimental system, increased callosal size and regularity is associated with greater hemispheric specialization.

Aging↗
PubMed1986

Oligodendrocyte production and myelin recovery in heterozygous jimpy mice: an autoradiographic study.

Jimpy is a genetic disorder of mouse resulting in hypomyelination. In this study oligodendrocyte proliferation was examined in heterozygous carriers of the jimpy gene. The incorporation of [3H]-thymidine into DNA is increased in jimpy heterozygotes compared to controls. An autoradiographic analysis indicated that oligodendrocytes are the predominant neuroglial cell type being produced in the brain at the ages studied in both heterozygotes and control animals. In addition, the total number of labeled oligodendrocytes was increased in the heterozygote animals compared to controls. These results, taken together, indicate that the rate of oligodendrocyte production is greater in jimpy heterozygotes than in control animals. We have previously shown that young jimpy heterozygotes have a reduced myelin content and older heterozygotes do not. The increased rate of oligodendrocyte production, demonstrated in this study, is most likely responsible for the increasing myelin content in the heterozygote. Further study of the cellular interactions which trigger oligodendrocyte production and myelin recovery in the jimpy heterozygote may be relevant to remyelination in other disease states, including those affecting humans.

Animals↗
PubMed1983

Myelin sheath thickness in the CNS is regulated near the axon.

Two myelin sheaths sharing a common outer tongue process are illustrated in a thin section electron micrograph from mouse optic nerve. Although they derive from the same outer tongue process, and therefore from the same oligodendrocyte, the two sheaths are of different thicknesses (6 and 9 turns). The example demonstrates that myelin sheath thickness is regulated independently for each axon, at a site very near the axon.

Animals↗
PubMed1983

Altered brain copper and zinc content in quaking mice.

Brain copper and zinc levels were determined in 21-day-old and "adult" C3HeB/FeJ quaking mice and in normal littermate controls. Expressed per gram dry weight of brain, copper was increased 84% over normal mice at 21 days after birth, but was not significantly different from normal in the adults. Zinc was increased 23 to 24% at both ages. At both ages, brains from quaking mice had a significantly reduced content of solids, indicating increased water content in the mutant brain. Our study is the first to report copper and zinc content as a measure of both wet and dry brain weights. Our results indicate abnormal copper content in the quaking mutant. The relationship between copper content and other aspects of the quaking phenotype, including its seizure behavior and myelin deficit, remain to be established.

Aging↗
PubMed1982

Synaptogenesis in chick paravertebral sympathetic ganglia: a morphometric analysis.

Synaptogenesis was studied in lumbar sympathetic ganglia of chicken by light and electron microscopic morphometric methods. At 10 days in ovo, fewer than 1% of the adult number of synapses are present. The total numbers of synapses and of synaptic vesicles per ganglion increase progressively with age; however, the majority of both are formed after 30 days after hatching. The average number of synaptic vesicles per synapse increases several fold after hatching. The numbers of synapses and of synaptic vesicles per ganglion increase roughly in concert with biochemical markers of presynaptic development (activity of choline acetyltransferase and levels of acetylcholine) as well as postsynaptic development (tyrosine hydroxylase; based on biochemical data reported elsewhere). The amount of acetylcholine and activity of choline acetyltransferase per synaptic vesicle at 10 days in ovo are 8 and 27 times the corresponding adult values. By 1 day after hatching, these ratios have fallen to near adult levels. These data are consistent with the early presence of cholinergic neuroblasts, as suggested by others, and suggest further that such cholinergic neuroblasts are eliminated, or their cholinergic properties suppressed, before hatching.

Animals↗
PubMed1982

Recovery of myelination in rat optic nerve after developmental retardation by cortisol.

Oligodendrocyte formation and myelination in the optic nerve of rats treated with cortisol on postnatal days 7 and 18 were investigated at 21 and 60 days by autoradiographic and morphometric methods. At 21 days, the amount of myelin in the optic nerve of treated rats was reduced by 42%. This reduction was accompanied by a 39% decrease in the number of myelinated axons. In addition, the myelin/axon area ratio was reduced 22% for those axons which were myelinated. At 60 days, the amount of myelin, the number of axons myelinated, the average axonal size, and the average amount of myelin per axon had completely recovered to normal values. Tritiated thymidine-labeling experiments showed that the genesis of oligodendrocytes was enhanced following the cessation of treatment. Since the number of oligodendrocytes in the optic nerve of treated rats was normal at 60 days, it is suggested that the retarding effect of cortisol on myelination in the optic nerve may be mediated, at least in part, by inhibited formation of oligodendrocytes during treatment.

Aging↗
PubMed1980

Fine structure of granule cells and related interneurons (termed Golgi cells) in the cochlear nuclear complex of cat, rat and mouse.

This paper describes the fine structure of granule cells and granule-associated interneurons (termed Golgi cells) in the cochlear nuclei of cat, rat and mouse. Granule cells and Golgi cells are present in defined regions of ventral and dorsal cochlear nuclei collectively termed "cochlear granule cell domain'. The granule cells are small neurons with two or three short dendrites that give rise to a few branches with terminal expansions. These participate in glomerular synaptic arrays similar to those of the cerebellar cortex. In the glomeruli the dendrites form short type 1 synapses with a large, centrally-located mossy bouton containing round synaptic vesicles and type 2 synapses with peripherally located, smaller boutons containing pleomorphic vesicles. The granule cell axons is thin and beaded and, on its way to the molecular layer of the DCN, takes a straight course, which in ventral nucleus is parallel to the pial surface. Neurons of the second category resemble cerebellar Golgi cells and occur everywhere interspersed among the granule cells. They are usually larger than the granule cells and give rise to dendrites which may branch close to and curve around the cell body. The dendrites contain numerous mitochondria and are laden with thin appendages, giving them a hairy appearance. Both the cell body and the stem dendrites participate in glomerular synaptic arrays. Golgi cell glomeruli are distinguishable from the granule cell glomeruli by unique features of the dendritic profiles and by longer, type 1 synaptic junctions with the central mossy bouton. The Golgi cell axon forms a beaded plexus close to the parent cell body. The synaptic vesicle population of the mossy boutons suggests that they are a heterogeneous group and may have multiple origins. Apparently, each of the various classes participates in both granule and Golgi cell glomeruli. The smaller peripheral boutons with pleomorphic vesicles in the two types of glomeruli may represent Golgi cell axons which make synaptic contacts with both granule and Golgi cells. The Golgi cell axons which make synaptic contacts with both granule and Golgi cells. The Golgi cell dendrites, on the other hand, are also contacted by small boutons en passant with round synaptic vesicles, which may represent granule cell axons. A tentative scheme of the circuitry in the cochlear granule cell domain is presented. The similarity with the cerebellar granule cell layer is striking.

Animals↗
PubMed1979

The fine structure of the feline superior vestibular nucleus: identification and synaptology of the primary vestibular afferents.

The superior vestibular nucleus of the cat and its primary vestibular efferents were examined by light and electron microscopy. The primary vestibular afferents branch within the nucleus in a sheet-like pattern, in the transverse plane. The dendritic fields of many secondary neurons are shaped like discs and are also oriented in the transverse plane. This relation between the primary afferents and dendritic fields may be relevant to the convergence of primary afferents innervating particular endorgans onto secondary neurons. Synaptic boutons in the SV were divided into 3 putative types on the basis of the size and shape of their synaptic vesicles. The primary afferent bouton was identified by comparing the SV of the two sides after unilateral lesions of the vestibular ganglion. Its boutons contain round vesicles of 40 nm average diameter and are associated with prominent postsynaptic densities; the two other putative bouton types contain smaller, round vesicles, and pleomorphic vesicles. The primary afferent boutons largely contact proximal dendrites, their appendages, and cell somata of the secondary neurons. In animals receiving unilateral lesions of the vestibular ganglion and allowed to survive long enough for the primary afferent boutons to disappear (5--6 days), there occurs in the denervated as compared to normal SV: (1) a decrease in the fraction of the somal surface of the secondary neurons covered by boutons with small round vesicles; and (2) a decrease in the ratio: number of boutons with small round vesicles to number of boutons with pleomorphic vesicles. In addition, there appears on the lesioned side a new group of boutons with pleomorphic vesicles smaller than those in boutons from the control side. These observations suggest plastic changes in response to deafferentation, and may be related to the marked behavioral recovery which occurs within a few days after lesion of the vestibular ganglion.

Afferent Pathways↗